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Cell. 1994 Apr 8;77(1):41-51.

Evidence that random and imprinted Xist expression is controlled by preemptive methylation.

Author information

1
Section of Comparative Biology, Medical Research Council Clinical Research Centre, Harrow, England.

Abstract

The mouse Xist gene is expressed exclusively from the inactive X chromosome and may control the initiation of X inactivation. We show that in somatic tissues the 5' end of the silent Xist allele on the active X chromosome is fully methylated, while the expressed allele on the inactive X is completely unmethylated. In tissues that undergo imprinted paternal Xist expression and imprinted X inactivation, the paternal Xist allele is unmethylated, and the silent maternal allele is fully methylated. In the male germline, a developmentally regulated demethylation of Xist occurs at the onset of meiosis and is retained in mature spermatozoa. This may be the cause of imprinted expression of the paternal Xist allele. A role for methylation in the control of Xist expression is further supported by the finding that in differentiating embryonic stem cells during the initiation of X inactivation, differential methylation of Xist alleles precedes the onset of Xist expression.

PMID:
8156596
DOI:
10.1016/0092-8674(94)90233-x
[Indexed for MEDLINE]

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